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are-Earth Chain-Based Metal–Organic Frameworks with a Pyrene Linker and Their Performance in the Detoxification of a Mustard Gas Simulant

The date of: 2026-07-01
viewed: 3

来源:ACS Publications

In this work, the pyrene-based linker 1,3,6,8-tetrakis(p-benzoic acid)pyrene (H4TBAPy) is used for the synthesis of rare-earth (RE) metal–organic frameworks (MOFs) featuring chain-based secondary building units with Y(III) and the series of 15 lanthanoids, yielding two different MOFs. One named RE-CU-05 with Y(III) and Gd(III) to Lu(III) and the second named RE-CU-06 with La(III) to Eu(III). Synchrotron X-ray diffraction measurements were used to determine the local structure of the nine RE-CU-05 analogues through pair distribution function (PDF) analysis, while electron diffraction (ED) and Rietveld refinement were used for structure solution of the six RE-CU-06 analogues. RE-CU-05 and RE-CU-06 were studied for the selective photooxidation of the sulfur mustard simulant 2-chloroethyl ethyl sulfide to 2-chloroethyl ethyl sulfoxide, achieving over 98% conversion in 10 min (La-CU-06) or 15 min (Tb-, Tm- and Yb-CU-05), with half-lives of 3.4 and 4.6 min for La-CU-06 and Tb-CU-05, respectively. These half-lives are competitive with those reported for other pyrene-based MOFs with much larger BET areas such as RE-CU-10 and Zr-NU-1000 under the same reaction conditions. The outstanding performance of RE-CU-05 and RE-CU-06 is attributed to the balance between chromophore density, pyrene-core spacing and orientation, surface area, and pore accessibility, which enables efficient light utilization and fast mass-transfer processes, highlighting the potential of chain-based MOFs as efficient photocatalysts.



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